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MSAT Technical Lead

Job in 4040, Basel, Kanton Basel-Landschaft, Switzerland
Listing for: R&D Partners
Full Time position
Listed on 2026-08-18
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, Quality Engineering
Salary/Wage Range or Industry Benchmark: 150000 - 210000 CHF Yearly CHF 150000.00 210000.00 YEAR
Job Description & How to Apply Below

Could your expertise in biologics development and manufacturing help optimise processes, improve yields, and shape the future of life-changing therapies?

R&D Partners is seeking a skilled professional to provide technical leadership in biologics development and manufacturing. In this role, you will oversee commercial and clinical programs, ensuring processes are validated, compliant, and ready for inspection. You will play a key role in optimizing processes, improving yields, and driving cost efficiency while collaborating with external manufacturing partners and regulatory bodies.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:
  • Lead technical aspects of biologics programs, ensuring compliance and readiness for inspections.
  • Manage mammalian cell culture operations, including cell banking, implementing new working cell banks, and qualifying scale-down models.
  • Oversee lifecycle management and execute projects to optimise processes, improve yields, and reduce costs.
  • Supervise technology transfer and scale-up activities with external manufacturing partners for clinical and commercial phases.
  • Contribute to regulatory documentation, including annual product reviews, registration files, variations, and responses to regulatory queries.
  • Govern external manufacturing by supervising technical studies, qualifications, validations, and evaluations of contract manufacturing organizations (CMOs).
  • Drive continuous improvement initiatives to enhance process reliability, robustness, and internal workflows.
Key Skills and Requirements:
  • Strong expertise in mammalian cell culture and upstream operations.
  • Experience with cell banking, scale-down model qualification, and new working cell bank implementation.
  • Knowledge of lifecycle management, process optimisation, and cost-efficiency strategies.
  • Familiarity with technology transfer, scale-up processes, and external manufacturing oversight.
  • Ability to contribute to regulatory documentation and respond to authority queries.
  • Proven ability to lead continuous improvement initiatives and enhance business processes.
  • Strong organisational, communication, and problem-solving skills.

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